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Donor Research Coordinator, Sr. jobs in District of Columbia

Donor Research Coordinator, Sr. identifies potential donors and evaluates their interests and capacity to give to the organization. Conducts research and prospecting to locate individuals aligning with the organization's values and mission. Being a Donor Research Coordinator, Sr. analyzes data for trends and creates donor profiles to assist with donor development, stewardship, and direct communications and fundraising strategy. Uses a database or Customer Relationship Management (CRM) system to maintain research data and donor records, execute mailing or e-mail campaigns, and create reports. Additionally, Donor Research Coordinator, Sr. maintains confidentiality and complies with data privacy regulations and policies. Requires a bachelor's degree. Typically reports to a manager. The Donor Research Coordinator, Sr. work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. To be a Donor Research Coordinator, Sr. typically requires 4-7 years of related experience. (Copyright 2024 Salary.com)

Recently Added Donor Research Coordinator, Sr. jobs

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Sr Clinical Research Coordinator
  • Children's National Medical Center
  • Washington, DC FULL_TIME
  • Description The Senior Clinical Research Coordinator independently leads day-to-day operations of clinical research studies conducted by a principal investigator with limited supervision. In addition, the individual performs a variety of complex duties involved in the collection, compilation, documentation and analysis of clinical research data. The Senior Clinical Research Coordinator will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA) regulations. This individual may support multiple investigators with clinical and translational research projects and direct the work of a Clinical Research Assistant and Clinical Research Coordinator as assigned.
    Qualifications Minimum Education
    Bachelor's Degree B.A./B.S. degree in a science, technical, health-related field or other applicable discipline with at least 3 years of relevant experience (Required) Or
    Master's Degree Master's degree with at least 2 years of relevant experience (Required)

    Minimum Work Experience
    3 years At least 3 years of experience with a bachelor's degree. (Required) Or
    2 years At least 2 years of experience with a master's degree. (Required)

    Required Skills/Knowledge
    Knowledge of clinical research designs and needed infrastructure.
    Familiarity with databases, data collection tools and data analysis methods.
    Ability to manage multiple complex activities while maintaining close attention to detail and not losing sight of the organizational mission.
    Interpersonal skills that demonstrate formal and informal leadership in a diverse professional environment.

    Required Licenses and Certifications
    Internal candidates: Certification as a Clinical Research Professional (CCRP) through the Society of Clinical Research Associates (SoCRA) or equivalent research certification. Upon Hire (Required)
    External candidates: Certification as a Clinical Research Professional (CCRP) through the Society of Clinical Research Associates (SoCRA) or equivalent research certification within one year of hire. 1 Year (Required)

    Functional Accountabilities
    Responsible Conduct of Research
    • Consistently demonstrates adherence to the standards for the responsible conduct of research.
    • Plans, conducts and manages research projects within federal and institutional regulations and policies under the direction of the principal investigator.
    • Stays informed of and adheres to institutional policies, and federal regulations (e.g. Titles 21 and 45 of the Code of Federal Regulations) and guidances (International Counsel on Harmonization) regarding human subjects' research and use of protected health information.
    • Uses research funds and resources appropriately.
    • Maintains confidentiality of data as required.
    • Meets all annual job-related training and compliance requirements.
    Research Administration
    • Maintains knowledge and comprehension of assigned research protocols, including study procedures, timelines and eligibility.
    • Accurately creates, completes, maintains, organizes and accounts for study materials, including participant lists and visit logs, regulatory binders, case report forms, laboratory kits, investigational product(s) and participation incentives.
    • Uses and accounts for research funds and resources at performance level, including reconciling research subject billing if assigned.
    • Attends study meetings, which could include overnight travel, as requested by principal investigator.
    • Works well with other members of the research team, appreciates a diverse workplace and seeks and provides input when appropriate.
    • Serves as an effective liaison between the investigators, sponsors, hospital departments involved with research studies and the Clinical Research Center.
    • Identifies and resolves issues and challenges with appropriate input and oversight.
    • Reviews journals, abstracts and scientific literature to obtain information relevant to clinical research programs.
    • Creates standard operating procedures (SOPs), and implements operational plans.
    • Provides oversight and training to study team members for a variety of studies.
    • Develops study documents, including consent forms and protocols.
    Participant Enrollment
    • Adheres to the IRB-approved recruitment plan.
    • Screens subjects for eligibility per the protocol and institutional policies.
    • Communicates effectively and provides information to a diverse, vulnerable subject population in accordance with institutional policies.
    • Interacts with study participants and/or legally authorized representatives (LARs) to communicate study purpose and participation details and to assess participation interest.
    • Engages participants/LARs in the informed consent process according to institutional policies.
    Study Management
    • Conducts/participates in feasibility assessments to ensure adequate site resources and infrastructure are available for protocol participation.
    • Plans, conducts and manages research activities in accordance with federal regulations and guidance documents and sponsor and institutional policies under the direction of a senior study team member.
    • Ensures regulatory integrity of protocols through the accurate and timely preparation and submission of documents and reports to the sponsor, IRB and other oversight bodies in accordance with federal regulations, sponsor SOPs and institutional policies.
    • Authors study submissions and related documents based on functional role; this may include IRB contingency responses, ClinicalTrials.gov postings, Certificate of Confidentiality applications and scholarly presentations and publications.
    • Registers and records participant visits in the appropriate tracking system.
    • Anticipates study needs and subject caseload to meet organizational objectives and deadlines in a timely manner.
    • Coordinates, prepares for and responds to routine oversight body visits and audits.
    • Independently authors reports to oversight bodies and/or trains and oversees staff performing these tasks.
    Data Collection
    • Ensures data is collected as required by protocol and in accordance with research data principles (ALCOAC: Attributable, Legible, Contemporaneous, Original, Accurate and Complete).
    • Ensures that queries are resolved within sponsor and institutional timelines.
    • Plans and performs research specimen collection, labeling and storage/shipping if assigned; maintains accurate sample accountability/chain of custody documentation.
    • Ensures secure storage of study documents.

    Organizational Accountabilities
    Organizational Accountabilities (Staff)
    Organizational Commitment/Identification
    • Anticipate and responds to customer needs; follows up until needs are met

    Teamwork/Communication
    • Demonstrate collaborative and respectful behavior
    • Partner with all team members to achieve goals
    • Receptive to others' ideas and opinions

    Performance Improvement/Problem-solving
    • Contribute to a positive work environment
    • Demonstrate flexibility and willingness to change
    • Identify opportunities to improve clinical and administrative processes
    • Make appropriate decisions, using sound judgment

    Cost Management/Financial Responsibility
    • Use resources efficiently
    • Search for less costly ways of doing things

    Safety
    • Speak up when team members appear to exhibit unsafe behavior or performance
    • Continuously validate and verify information needed for decision making or documentation
    • Stop in the face of uncertainty and takes time to resolve the situation
    • Demonstrate accurate, clear and timely verbal and written communication
    • Actively promote safety for patients, families, visitors and co-workers
    • Attend carefully to important details - practicing Stop, Think, Act and Review in order to self-check behavior and performance
    Primary Location: District of Columbia-Washington
    Work Locations:
    CN Hospital (Main Campus)
    111 Michigan Avenue
    Washington 20010
    Job: Research
    Organization: Ctr Neuroscience & Behav Med
    Position Status: R (Regular) - FT - Full-Time
    Shift: Day
    Work Schedule: M-F 8:30am-5pm
    Job Posting: Mar 11, 2024, 6:32:16 PM

    Equal Opportunity Employer of Minorities, Females, Protected Veterans, and Individual with Disabilities.

     

  • 1 Month Ago
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Research Data Coordinator
  • Greenwald Research
  • Washington, DC FULL_TIME
  • We are in search of a highly organized, communicative, and detail-oriented problem-solver to support the technical execution of market research projects from start to finish. You will work closely wit...
  • 8 Days Ago
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Sr Clinical Research Coordinator - Orthopedics
  • Children's National Medical Center
  • Washington, DC FULL_TIME
  • Description The Senior Clinical Research Coordinator independently leads day-to-day operations of clinical research studies conducted by a principal investigator with limited supervision. In addition,...
  • 23 Days Ago
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Coordinator, Donor Relations
  • The National Park Foundation
  • Washington, DC FULL_TIME
  • Reporting to the Senior Director, Donor Relations, the Coordinator, Donor Relations is an essential part of the Philanthropy team, working to create an outstanding experience for donors at the Nationa...
  • 1 Month Ago
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Facilities Coordinator
  • Cornerstone Research
  • Washington, DC OTHER
  • Overview FACILITIES COORDINATOR (ON-SITE – WASHINGTON, DC) If you are passionate about the day-to-day operations of maintaining a facility and enjoy providing exceptional client service to your fellow...
  • 1 Month Ago
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Accounts Receivable Coordinator
  • Cornerstone Research
  • Washington, DC OTHER
  • Overview ACCOUNTS RECEIVABLE COORDINATOR (HYBRID - WASHINGTON, DC) If you are an accounting professional looking for an opportunity to showcase your accuracy and attention to detail, then we would lik...
  • 1 Month Ago
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Donor Research Coordinator, Sr. jobs at Popular Companies

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Research Coordinator
  • NYU Langone Health
  • New York, NY
  • NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of...
  • 4/23/2024 12:00:00 AM
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Research Coordinator - Research Operations
  • Denver Health
  • Denver, CO
  • We are recruiting for a Research Coordinator - Research Operations to join our team! We are here for life's journey. Whe...
  • 4/22/2024 12:00:00 AM
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Research Coordinator (Research Professional 3)
  • University of Minnesota
  • Minneapolis, MN
  • About the Job Job Duties/Responsibilities: * Screen and recruit clinical trial subjects by pre-screening clinic patients...
  • 4/22/2024 12:00:00 AM
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Clinical Research Coordinator/ Research Nurse
  • M3 Global Research
  • Durham, NC
  • Company Description M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meetin...
  • 4/22/2024 12:00:00 AM
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Clinical Research Coordinator (Research Professional 1)
  • University of Minnesota
  • Minneapolis, MN
  • About the Job The primary purpose of the Clinical Research Coordinator (Research Professional 1) position includes: cond...
  • 4/22/2024 12:00:00 AM
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Community Outreach Research Coordinator/Research Associate - Administrative
  • Compu-Vision Consulting, Inc.
  • Santa Monica, CA
  • Title: Community Outreach Research Coordinator Location: 1399 S Roxbury Drive, Suite 100, Los Angeles, CA 90035 Duration...
  • 4/20/2024 12:00:00 AM
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Research Coordinator
  • NYU Langone Health
  • New York, NY
  • NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of...
  • 4/20/2024 12:00:00 AM
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Research Coordinator
  • Leidos
  • San Diego, CA
  • Description Are you looking for a career that will make an impact? The Leidos Military and Veterans Health Solutions Ope...
  • 4/9/2024 12:00:00 AM
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About District of Columbia

Washington, D.C. is located in the mid-Atlantic region of the U.S. East Coast. Due to the District of Columbia retrocession, the city has a total area of 68.34 square miles (177.0 km2), of which 61.05 square miles (158.1 km2) is land and 7.29 square miles (18.9 km2) (10.67%) is water. The District is bordered by Montgomery County, Maryland to the northwest; Prince George's County, Maryland to the east; Arlington County, Virginia to the south; and Alexandria, Virginia to the west. The south bank of the Potomac River forms the District's border with Virginia and has two major tributaries: the An...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Donor Research Coordinator, Sr. jobs
$85,817 to $115,450

Most Popular Cities in District of Columbia for Donor Research Coordinator, Sr. Jobs

What does a Donor Research Coordinator, Sr. do?

Donor Research Coordinator, Sr. in Eugene, OR
Write highly personalized correspondences to high-level donors to recognize and communicate the impact of their contributions to the BSO.
February 18, 2020
Donor Research Coordinator, Sr. in Corpus Christi, TX
Additionally, you will participate in team the utilization of system reports, donor information updates, records maintenance, and limited gift entry.
November 30, 2019
Donor Research Coordinator, Sr. in Philadelphia, PA
You will support the varied goals of the team primarily focusing on accurate and timely tax receipt and donor acknowledgment correspondence to properly express gratitude for each donor’s contributions to the BSO.
November 29, 2019